Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07091825

Evaluating the Efficacy and Safety of Contact Lens Lubricant in Rigid Gas Permeable Corneal Contact Lens Wearers

A Prospective, Multi-center, Open-Label, Randomized Controlled, Non-Inferiority Clinical Study Evaluating the Efficacy and Safety of Contact Lens Lubricant in Rigid Gas Permeable Corneal Contact Lens Wearers

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
152 (estimated)
Sponsor
Avizor SA · Industry
Sex
All
Age
8 Years
Healthy volunteers
Not accepted

Summary

This trial aims to evaluate the safety and effectiveness of LACRIFRESH OCU-DRY 0.3% OSD, a contact lens lubricant produced by AVIZOR, S.A. This clinical trial adopts a Multi-center, randomized, open-label, positive parallel-controlled design in accordance with the principles outlined in the Norms on the Quality Management for the Clinical Trials of Medical Devices issued by the National Medical Products Administration of China. Meanwhile, following statistical requirements, 152 rigid contact lens wearers are planned to be enrolled after screening and meeting the inclusion criteria. Participants will be randomly assigned to groups and provided with lenses, lubricants, and care solutions accordingly. Clinical follow-up assessments are scheduled at 1 week, 1 month, and 3 months after use. The primary efficacy indexes are the percentage of patients with binocular comfort score ≥ Level 3 at the 1-month follow-up and the percentage of patients with best corrected distance visual acuity with contact lenses for both eyes ≥5.0 at the 1-month follow-up after using the contact lens lubricant. Secondary efficacy indexes include, best corrected distance visual acuity with lenses, visual acuity with lenses, residual diopter, tear break-up time, uncorrected visual acuity, examination of contact lens fitting status, lens assessment, and contact lens lubricant evaluation during the corresponding follow-up periods. Safety indexes include slit lamp examination, fundus examination, IOP, corneal endothelial cell, adverse events, serious adverse events, device defects that may lead to serious adverse events, other device defects during the corresponding follow-up periods.

Conditions

Interventions

TypeNameDescription
DEVICELACRIFRESH OCU-DRY 0.3% OSDUse LACRIFRESH OCU-DRY 0.3% OSD as the daily contact lens lubricant product.
DEVICERigid contact lens lubricantUse Rigid contact lens lubricant as the daily contact lens lubricant product.

Timeline

Start date
2025-06-27
Primary completion
2026-03-30
Completion
2026-06-30
First posted
2025-07-29
Last updated
2025-07-29

Locations

3 sites across 1 country: China

Source: ClinicalTrials.gov record NCT07091825. Inclusion in this directory is not an endorsement.